Top Clinical Research Executive jobs in New Hampshire
Top Clinical Research Executive plans and directs all aspects of the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Top Clinical Research Executive ensures adherence to SOPs, Good Clinical Practice and FDA regulations. Requires an advanced degree. Additionally, Top Clinical Research Executive typically reports to top management. The Top Clinical Research Executive manages a departmental function within a broader corporate function. Develops major goals to support broad functional objectives. Approves policies developed within various sub-functions and departments. To be a Top Clinical Research Executive typically requires 8+ years of managerial experience. Comprehensive knowledge of the overall departmental function. (Copyright 2024 Salary.com)
Recently Added Top Clinical Research Executive jobs
Clinical Research Coordinator
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
-
Department: Operations
Employment Type: Full Time
Location: ActivMed Practices & Research | Portsmouth, NH
Reporting To: Christopher Lenox
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
Key Responsibilities
In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under The Direction Of The Site Manager/Director And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With FDA, GCP, ICH Regulations And Guidelines- Screening of patients for study enrollment;
- Patient consents;
- Patient follow-up visits;
- Documenting in source clinic charts;
- Entering data in EDC and answers queries;
- Obtaining vital signs and ECGs;
- May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
- Requesting and tracking medical record requests;
- Updating and maintaining logs, chart filings;
- Maintaining & ordering study specific supplies;
- Scheduling subjects for study visits and conducts appointment reminders;
- Building/updating source as needed;
- Conducting monitoring visits and resolves issues as needed in a timely manner;
- Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
- Filing SAE/Deviation reports to Sponsor and IRB as needed;
- Documenting and reporting adverse events;
- Reporting non-compliance to appropriate staff in timely manner;
- Maintaining positive and effective communication with clients and team
- Always practicing ALCOAC principles with all documentation;
- Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
- Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
- Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
- Assist with training of new research assistants and coordinators;
- Assist with scheduling and planning for visit capacity for assigned studies;
- May set up, train and maintain all technology needed for studies;
- May assist with study recruitment, patient enrollment, and tracking as needed;
- May handle more complex study assignments and volumes;
- May participate in community outreach / education events;
- Maintaining confidentiality of patients, customers and company information, and;
- Performing all other duties as requested or assigned.
Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 2 years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills- Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
- Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
- Strong organizational skills and attention to detail.
- Well-developed written and verbal communication skills.
- Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
- Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
- Must be professional, respectful of others, self-motivated, and have a strong work ethic.
- Must possess a high degree of integrity and dependability.
- Ability to work under minimal supervision, identify problems and implement solutions.
- Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.
- Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
- Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
- 5 Days Ago
Clinical Research Assistant / EMT
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
- 11 Days Ago
Clinical Research Assistant / Medical Assistant
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
- 4 Days Ago
Medical Assistant / Clinical Research Assistant
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Medical Assistant / Clinical Research AssistantDepartment: Operations Employment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanz...
- 20 Days Ago
Clinical Research Patient Recruiter (Patient Registrar) - onsite
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Clinical Research Patient Recruiter (Patient Registrar) - onsiteDepartment: Patient Recruitment Employment Type: Full TimeLocation: ActivMed Practices & Research | Pease, NHDescriptionAlcanza is a gro...
- 26 Days Ago
Clinical Reseach Site Manager
- Alcanza Clinical Research
-
Portsmouth, NH
FULL_TIME
- Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Pease, NHReporting To: Joanne MonaghanDescriptionAlcanza is a growing multi-site, multi-phase clinical researc...
- 4 Days Ago
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-
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Research Professional
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-
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Investment Research Professional
- Leadenhall Search & Selection
-
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Research Staff Assistant
- Columbia University
-
New York, NY
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Coord Clinical Research II - Clinical Research Staff
- MetroHealth
-
Cleveland, OH
- **Location:** **METROHEALTH MEDICAL CENTER** **Biweekly Hours:** **80.00** **Shift:** **8-4:30** **The MetroHealth Syste...
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Clinical Research Coordinator (Research Professional 1)
- University of Minnesota
-
Minneapolis, MN
- About the Job We are seeking a motivated and detail-oriented Clinical Research Coordinator (Research Professional 1) to ...
- 6/7/2024 12:00:00 AM
About New Hampshire
New Hampshire is part of the six-state New England region. It is bounded by Quebec, Canada, to the north and northwest; Maine and the Atlantic Ocean to the east; Massachusetts to the south; and Vermont to the west. New Hampshire's major regions are the Great North Woods, the White Mountains, the Lakes Region, the Seacoast, the Merrimack Valley, the Monadnock Region, and the Dartmouth-Lake Sunapee area. New Hampshire has the shortest ocean coastline of any U.S. coastal state, with a length of 18 miles (29 km), sometimes measured as only 13 miles (21 km). New Hampshire was home to the rock forma...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Top Clinical Research Executive jobs
$215,271 to $392,885